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在转基因小鼠中表达由与SV40 T抗原基因相连的小鼠生长激素释放激素基因启动子组成的融合基因。

Expression of a fusion gene consisting of the mouse growth hormone-releasing hormone gene promoter linked to the SV40 T-antigen gene in transgenic mice.

作者信息

Nogues N, Magnan E, De Grandis P, Butz M, Kineman R D, Kopchick J J, Frohman L A

机构信息

Department of Medicine, University of Illinois at Chicago, 60612, USA.

出版信息

Mol Cell Endocrinol. 1998 Feb;137(2):161-8. doi: 10.1016/s0303-7207(97)00242-6.

Abstract

Limited information is available concerning the regulation of growth hormone-releasing hormone (GHRH) gene expression in the hypothalamus, largely because of the lack of a suitable cellular model. In an attempt to immortalize hypothalamic GHRH-producing neurons, we have generated a transgenic mouse model which expresses the simian virus 40 (SV40) T-antigen gene (Tag) under the control of the GHRH gene promoter. The transgene contains approximately 5 kb of mouse GHRH gene sequences, including 3.5 kb of the 5'-flanking region, the entire hypothalamic exon 1 and 1.5 kb of intron 1, fused to the SV40 Tag gene. This construct was microinjected into fertilized oocytes. Fourteen of 96 mice born had integrated the transgene. These mice were fertile and showed no signs of central or peripheral tumors. The pattern of expression of the SV40 Tag gene was analyzed in four different transgenic lines by RT-PCR. The tissues tested include: hypothalamus, pituitary, cortex, cerebellum, spinal cord, adrenal, testis, spleen and lung. Transgene expression was consistently detected in the hypothalamus of all lines. In addition, SV40 Tag expression was also detected in the hypothalamus by Northern blot analysis in two of the transgenic lines. SV40 Tag expression was also detected in the testis of all transgenic lines by RT-PCR. This result was not expected since the GHRH gene sequences present in the transgene do not include the testis-specific transcription initiation site previously described. This suggests that GHRH gene expression in the mouse testis can be directed by regulatory sequences located downstream of the testis specific transcription start site. We conclude that the promoter region of the GHRH gene included in this construct contains the regulatory elements necessary to drive hypothalamic and testis expression in vivo. In addition, all mice from one of the transgenic lines developed cataracts in both eyes. SV40 Tag expression was detected not only in eyes with cataracts, but also, to a lesser extent, in eyes from other transgenic lines. Furthermore, the endogenous GHRH gene was found to be expressed in the eyes of normal mice.

摘要

关于下丘脑生长激素释放激素(GHRH)基因表达的调控,目前可用信息有限,这主要是因为缺乏合适的细胞模型。为了使下丘脑产生GHRH的神经元永生化,我们构建了一种转基因小鼠模型,该模型在GHRH基因启动子的控制下表达猿猴病毒40(SV40)T抗原基因(Tag)。转基因包含约5 kb的小鼠GHRH基因序列,包括3.5 kb的5'侧翼区域、整个下丘脑外显子1和1.5 kb的内含子1,与SV40 Tag基因融合。该构建体被显微注射到受精卵中。出生的96只小鼠中有14只整合了转基因。这些小鼠可育,未表现出中枢或外周肿瘤的迹象。通过RT-PCR分析了四个不同转基因品系中SV40 Tag基因的表达模式。检测的组织包括:下丘脑、垂体、皮质、小脑、脊髓、肾上腺、睾丸、脾脏和肺。在所有品系的下丘脑均持续检测到转基因表达。此外,通过Northern印迹分析在两个转基因品系的下丘脑中也检测到了SV40 Tag表达。通过RT-PCR在所有转基因品系的睾丸中也检测到了SV40 Tag表达。由于转基因中存在的GHRH基因序列不包括先前描述的睾丸特异性转录起始位点,所以这个结果出乎意料。这表明小鼠睾丸中的GHRH基因表达可由睾丸特异性转录起始位点下游的调控序列引导。我们得出结论,该构建体中包含的GHRH基因启动子区域含有在体内驱动下丘脑和睾丸表达所需的调控元件。此外,其中一个转基因品系的所有小鼠双眼均出现白内障。不仅在有白内障的眼睛中检测到了SV40 Tag表达,在其他转基因品系的眼睛中也检测到了程度较轻的表达。此外,发现正常小鼠的眼睛中内源性GHRH基因也有表达。

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